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Angewandte Genetik in der Pädiatrie

Monatsschrift Kinderheilkunde, 2018-09, Vol.166 (9), p.774-784

2018

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New Mutations Associated with Rasopathies in a Central European Population and Genotype–Phenotype Correlations

Annals of human genetics, 2016-01, Vol.80 (1), p.50-62

2016

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Evidence from a leukaemia model for maintenance of vascular endothelium by bone-marrow-derived endothelial cells

The Lancet (British edition), 2000-05, Vol.355 (9216), p.1688-1691

2000

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Therapeutic step-up strategy for management of hereditary pancreatitis in children

Journal of pediatric surgery, 2015-04, Vol.50 (4), p.511-514

2015

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Low concentrations of STI571 in the cerebrospinal fluid: a case report

British journal of haematology, 2002-06, Vol.117 (3), p.623-625

2002

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Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)

Ultraschall in der Medizin, 2015-10, Vol.36 (5), p.507-510

2015

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Planar embryos have poor prognosis in terms of blastocyst formation and implantation

Reproductive biomedicine online, 2012-09, Vol.25 (3), p.267-272

2012

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Lp(a) glycoprotein phenotypes: inheritance and relation to Lp(a)-lipoprotein concentrations in plasma

The Journal of clinical investigation, 1987-08, Vol.80 (2), p.458-465

1987

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Spontaneous remission in a secondary acute myelogenous leukaemia following invasive pulmonary aspergillosis

Annals of hematology, 2001-07, Vol.80 (7), p.423-425

2001

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Healthy twin live-birth after ionophore treatment in a case of theophylline-resistant Kartagener syndrome

Journal of assisted reproduction and genetics, 2015-06, Vol.32 (6), p.873-877

2015

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Prenatal diagnosis of de novo mosaic deletion 13q associated with multiple abnormalities

Ultrasound in obstetrics & gynecology, 2002-04, Vol.19 (4), p.396-399

2002

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Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH

Nature genetics, 1999-04, Vol.21 (4), p.357-358

1999

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Polychemotherapy combined with G-CSF-mobilized donor buffy coat transfusion for granulocytic sarcoma after allogeneic BMT for AML

Bone marrow transplantation (Basingstoke), 1997-05, Vol.19 (9), p.947-949

1997

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P19 Polar body based preimplantation genetic diagnosis for female translocation carriers in a public hospital in Austria

Reproductive biomedicine online, 2010, Vol.20, p.S29-S29

2010

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Contribution of Endothelial Cells of Hematopoietic Origin to Blood Vessel Formation

Circulation research, 2001-01, Vol.88 (1), p.e1-e1

2001

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Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

Human genetics, 1997-05, Vol.99 (5), p.596-601

1997

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P–083 Analysis of chromosomal segregation and interchromosomal effects (ICE) in sperms from balanced translocation carriers using fluorescence in situ hybridization (FISH) after sperm selector separation

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome

Journal of medical genetics, 1997-04, Vol.34 (4), p.309-313

1997

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Effect of noninvasive first trimester diagnosis on indications and results of chorion villi sampling

Ultraschall in der Medizin, 2012-06, Vol.33 (3), p.245

2012

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Circulating endothelial cells after transplantation

The Lancet (British edition), 2001-05, Vol.357 (9266), p.1449-1449

2001

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Characterisation of a collecting duct carcinoma by cytogenetic analysis and comparative genomic hybridisation

International journal of oncology, 1998-09, Vol.13 (3), p.461

1998

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Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)

Human genetics, 1996-06, Vol.97 (6), p.784-793

1996

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High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization

Immunogenetics (New York), 2001-09, Vol.53 (7), p.611-615

2001

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Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridization

International journal of oncology, 2001-12, Vol.19 (6), p.1263

2001

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Cloning, genomic sequence, and chromosome mapping of Scyb11, the murine homologue of SCYB11 (alias betaR1/H174/SCYB9B/I-TAC/IP-9/CXCL11)

Cytogenetic and genome research, 2000-01, Vol.88 (3-4), p.278-282

2000

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Angewandte Genetik in der Pädiatrie

New Mutations Associated with Rasopathies in a Central European Population and Genotype–Phenotype Correlations

Evidence from a leukaemia model for maintenance of vascular endothelium by bone-marrow-derived endothelial cells

Therapeutic step-up strategy for management of hereditary pancreatitis in children

Low concentrations of STI571 in the cerebrospinal fluid: a case report

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)

Planar embryos have poor prognosis in terms of blastocyst formation and implantation

Lp(a) glycoprotein phenotypes: inheritance and relation to Lp(a)-lipoprotein concentrations in plasma

Spontaneous remission in a secondary acute myelogenous leukaemia following invasive pulmonary aspergillosis

Healthy twin live-birth after ionophore treatment in a case of theophylline-resistant Kartagener syndrome

Prenatal diagnosis of de novo mosaic deletion 13q associated with multiple abnormalities

Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH

Polychemotherapy combined with G-CSF-mobilized donor buffy coat transfusion for granulocytic sarcoma after allogeneic BMT for AML

P19 Polar body based preimplantation genetic diagnosis for female translocation carriers in a public hospital in Austria

Contribution of Endothelial Cells of Hematopoietic Origin to Blood Vessel Formation

Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

P–083 Analysis of chromosomal segregation and interchromosomal effects (ICE) in sperms from balanced translocation carriers using fluorescence in situ hybridization (FISH) after sperm selector separation

Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome

Effect of noninvasive first trimester diagnosis on indications and results of chorion villi sampling

Circulating endothelial cells after transplantation

Characterisation of a collecting duct carcinoma by cytogenetic analysis and comparative genomic hybridisation

Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)

High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization

Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridization

Cloning, genomic sequence, and chromosome mapping of Scyb11, the murine homologue of SCYB11 (alias betaR1/H174/SCYB9B/I-TAC/IP-9/CXCL11)

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